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Trial · NCT07894120

Registered outcomes11

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryMain effectiveness indicators90 days after treatment
Overall clinical efficacy rate,Using the Fitzpatrick Skin Wrinkle and Elasticity Rating Scale, a four level evaluation was conducted on the improvement rate of wrinkles before and after treatment, based on the pre-treatment baseline: significant improvement, moderate improvement, mild improvement, and no improvement. ① Significant improvement: Wrinkle improvement rate\>75%; ② Moderate improvement: The wrinkle improvement rate is between 51% and 75%; ③ Mild improvement: The wrinkle improvement rate is between 25% and 50%; ④ No improvement: Wrinkle improvement rate\<25%. Overall clinical efficacy rate=(number of significantly improved cases+number of moderately improved cases+number of mildly improved cases)/total cases.
PrimaryMain safety indicatorsBefore and immediately after treatmentMeasure the respiratory frequency of the subject using a pulmonary function meter,in beats per minute
PrimaryMain safety indicatorsBefore intervention, during treatment, and 90 days after treatmentAdverse event incidence rate
PrimarySecondary effectiveness indicatorsOn the 7th, 30th, and 90th day after treatmentVISIA Facial Rating
PrimarySecondary effectiveness indicatorsImmediately after treatmentVisual Analogue Scale
PrimarySecondary effectiveness indicatorsImmediately after treatment, 7 days after treatmentSkin reaction score
PrimarySecondary effectiveness indicators90 days after treatmentUsing a satisfaction rating scale,Calculate the proportion of satisfied patients
PrimaryMain safety indicatorsBefore and immediately after treatmentUsing a thermometer to measure the patient's body temperature,Body temperature unit Celsius
PrimaryMain safety indicatorsBefore and immediately after treatmentMeasure the subject's pulse using a pulse oximeter, in beats per minute
PrimaryMain safety indicatorsBefore and immediately after treatmentMeasure the subject's blood pressure using a sphygmomanometer, in mmHg
OtherSecondary safety indicatorsImmediately after treatmentEquipment failure rate

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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GET https://conductscience.org/api/trials/v1/NCT07894120/registered